Views and positions on current regulatory issues from the US FDA, the American Dental Association, the Italian Medical Device Manufacturers Association and many more now available in the August 2020 edition of the Journal of Medical Device Regulation

London, 11 August 2020 – The Journal of Medical Device Regulation releases today the contents of its August 2020 issue to non-subscribing readers.

The following articles are now publicly available through the Journal’s website – GlobalRegulatoryPress.com – 10 days after their official publication in the Journal:

• The US FDA summarises its recent programme changes designed to help improve consistency and efficiency in 510(k) reviews
• Where does artificial intelligence (AI) fit in regulatory frameworks?
• Developing cleaning instructions for reusable dental rotary cutting devices in the context of a risk analysis in the USA
• The rules governing the manufacturing of personalised medical devices in healthcare facilities
• Interpretation of Rule 21 of Regulation (EU) 2017/745 concerning medical devices composed of substances or a combination of substances

About the Journal of Medical Device Regulation

The Journal of Medical Device Regulation (founded in 2004) reaches regulatory professionals around the world and provides them with in-depth articles on current regulatory matters as well as topical information on international regulatory changes. In addition to publishing review and discussion articles by opinion leaders from the device community, the Journal summarises the global news headlines and provides useful reference information in the form of charts and briefing documents. The Journal is a quarterly, subscription-only publication that is available in electronic format.

For more information on the Journal of Medical Device Regulation, please contact us (tel: +44 7916 443811), email: sales@globalregulatorypress.com) or visit GlobalRegulatoryPress.com.